TY - JOUR
T1 - Fluorescent probes for the quantification of labile metal ions in living cells
AU - Kowada, Toshiyuki
AU - Mizukami, Shin
N1 - Funding Information:
This work was supported by JSPS KAKENHI (Nos. JP19K22241 and JP20K05702), and the Takeda Science Foundation, the Nakatani Foundation, and the “Dynamic Alliance for Open Innovation Bridging Human, Environment and Materials” Research Program in the “Network Joint Research Center for Materials and Devices”. We also acknowledge all of our collaborators shown in the original papers for their great contributions to the success of our studies.
Publisher Copyright:
© 2021 Society of Synthetic Organic Chemistry. All rights reserved.
PY - 2021/11/1
Y1 - 2021/11/1
N2 - Recent studies have revealed that some intracellular metal ions other than Ca2+ also act as signaling mediators. Detailed analyses of such intracellular metal ion dynamics will enhance our understanding of the physiological roles of these metal ions. Fluorescence imaging is a powerful technique for this purpose owing to its high spatiotemporal resolution. However, with respect to metal ion selectivity, subcellular localization, and robustness to intracellular environmental changes, there are not yet enough fluorescent metal–ion probes suitable for such intracellular analysis. Recently, we have developed several metal ion probes that combine the characteristics of small–molecule fluorescent probes, such as ease of tuning of fluorescence properties and metal ion affinities, with subcellular localizability by a tag protein. In this account, we introduce our recent achievements in the development of small molecule–protein hybrid fluorescent probes and their applications such as long–term imaging of intracellular Mg2+ dynamics and quantification of labile Zn2+ concentration in the Golgi apparatus.
AB - Recent studies have revealed that some intracellular metal ions other than Ca2+ also act as signaling mediators. Detailed analyses of such intracellular metal ion dynamics will enhance our understanding of the physiological roles of these metal ions. Fluorescence imaging is a powerful technique for this purpose owing to its high spatiotemporal resolution. However, with respect to metal ion selectivity, subcellular localization, and robustness to intracellular environmental changes, there are not yet enough fluorescent metal–ion probes suitable for such intracellular analysis. Recently, we have developed several metal ion probes that combine the characteristics of small–molecule fluorescent probes, such as ease of tuning of fluorescence properties and metal ion affinities, with subcellular localizability by a tag protein. In this account, we introduce our recent achievements in the development of small molecule–protein hybrid fluorescent probes and their applications such as long–term imaging of intracellular Mg2+ dynamics and quantification of labile Zn2+ concentration in the Golgi apparatus.
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U2 - 10.5059/YUKIGOSEIKYOKAISHI.79.1020
DO - 10.5059/YUKIGOSEIKYOKAISHI.79.1020
M3 - Article
AN - SCOPUS:85119996992
SN - 0037-9980
VL - 79
SP - 1020
EP - 1032
JO - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
JF - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
IS - 11
ER -